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GRHL3-related orofacial clefting

MONDO:0100579

Any orofacial clefting in which the cause of the disease is a mutation in the GRHL3 gene.

1 clinical trial for this condition and its sub-types, 0 tagged with GRHL3-related orofacial clefting itself.

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↑ Orofacial cleft (69)
Including sub-types (1) Tagged with GRHL3-related orofacial clefting (0)
Completed 1
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